Effects of sleep disturbance, cancer-related fatigue, and psychological distress on breast cancer patients’ quality of life: a prospective longitudinal observational study

More attention has gone to researching the cancer-related fatigue (CRF)–sleep disturbance (SD)–psychological distress (PD) symptom cluster in breast cancer patients during the chemotherapy period, but the change trend and heterogeneous development track in the whole treatment stage remain unclear, and it is also unclear whether the appearance of and changes in one symptom cause changes in other symptoms and quality of life (QoL). This study, using breast cancer patients’ data collected through a validated questionnaire, examined the relationships between SD, CRF, PD, and QoL using latent growth modeling analyses. CRF developmental trajectories showed an upward trend over five surveys (slope = 0.649, P < 0.001); PD showed a significant weakening trend (slope = − 0.583, P < 0.001); SD showed an increasing trend (slope = 0.345, P < 0.001), and QoL showed a statistically significant weakening trend (slope = − 0.373, P < 0.001). The initial CRF (coefficient = − 0.233, P < 0.01), PD (coefficient = − 0.296, P < 0.01), and SD (coefficient = − 0.388, P < 0.001) levels had a statistically significant negative effect on initial QoL level. The linear development rate of PD was statistically significant and negatively affected that of QoL (coefficient = − 0.305, P < 0.05), whereas the quadratic development rate of SD negatively affected that of QoL (coefficient = − 0.391, P < 0.05). Medical staff should identify the change characteristics of different variables based on SD, CRF, PD, and QoL change trajectories, and advance the intervention time, as changes in variables affect other variables’ subsequent changes.


Procedures
The research team included breast surgery and oncology physicians and nurses.The researchers obtained the consent and support of the relevant departments of the five hospitals, then contacted the follow-up nurses in the breast surgery and breast oncology departments of each hospital, and finally conducted online training.The researchers maintained real-time contact with the follow-up nurses in each hospital through WeChat, to address any issues that arose during follow-up.Each study participant completed their surgery and chemotherapy at the same hospital.When physicians found breast cancer cases that met the recruitment criteria in the first outpatient clinic, they obtained patients' informed consent, and then included them in the research group for follow-up management.After the patients were enrolled, the follow-up nurses established a follow-up database and were responsible for tracking the diagnosis, operation, date of chemotherapy, and chemotherapy plan, and they sent this data to the researchers, who made a follow-up plan.Data collection was mainly conducted by follow-up nurses in each hospital.After data collection at each stage was completed, the original data were packaged and sent to the researchers by the follow-up nurses for unified management.The researchers participated in quality control, regularly checked and adjusted the follow-up plan, and urged the follow-up nurses to complete the follow-up on time.
Five timepoints were selected for longitudinal tracking of patients' SD, CRF, PD, and QoL: within one week after initial cancer diagnosis (T1), within one week after the start of surgical treatment (T2), within one week after the end of all courses of chemotherapy (T3), six months after the end of chemotherapy (T4), and 12 months after the end of chemotherapy (T5).The researchers screened patients based on their outpatient medical records; conducted one-on-one, face-to-face, semi-structured interviews with those who met the criteria; and informed them of the study's purpose and follow-up arrangements.After patients were fully informed and had agreed to participate in this study, baseline data (T1) were collected: socio-demographic characteristics, disease-related data, SD, CRF, PD, and QoL.After the patients were discharged, dedicated follow-up phone calls were made during T2-T5, either at 09:00-11:00 or 16:00-18:00 h, to investigate the patients' SD, CRF, PD, and QoL status.
To reduce loss at follow-up, small gifts were distributed during the follow-up period, and each patient received a free physical examination.This study included as large a sample size as possible.

Sleep disturbance
The Pittsburgh sleep quality Index (PSQI), developed by Buysse 21 , was used to measure SD.The scale consists of 19 self-evaluated items and 5 other-evaluated items, of which only the first 18 self-evaluated items are scored (0-3 points) across seven dimensions: sleep quality, sleep latency, sleep duration, habitual sleep efficiency, SDs, use of sleep medicine, and daytime dysfunction.The total score across dimensions constitutes the total PSQI score (0-21 points).The higher the score, the worse the sleep quality; a total score > 7 indicates SD, while ≤ 7 indicates good sleep.The Cronbach's alpha values for the scale in this study is 0.89.

Cancer-related fatigue
The Chinese version of the Multidimensional Fatigue Symptom Inventory-Short Form (MFSI-SF) was used to measure CRF 22 .This is a self-report assessment composed of 27 items and five subscales: general fatigue, physical fatigue, emotional fatigue, mental fatigue, and vigor.For the four fatigue subscales, each item is assessed on a 5-point scale from 0 (not at all) to 4 (extremely serious); whereas for vigor, it is assessed from 0 (nearly always) to 4 (never).The total score is thus 0-108, with higher scores indicating more CRF.This instrument has excellent psychometric properties in the Chinese context 22 .The Cronbach's alpha values for the scale in this study is 93.

Psychological distress
The Distress Thermometer recommended by the National Comprehensive Cancer Network 23 was used to measure patients' PD.It is a self-evaluation tool, scored from 0 (no distress) to 10 (extreme distress).A Distress Thermometer score ≥ 4 indicates moderate to severe PD; < 4 indicates normal mood swings, with no special intervention required.Zhang et al. 24 found that the Distress Thermometer had excellent psychometric properties for China.

Quality of life
QoL was measured using the Functional Assessment of Cancer Therapy-Breast (FACT-B) 25 , composed of 36 items and five subscales: physiological, social/family, emotional, functional status, and additional concerns about breast cancer.Items are scored on a 5-point scale from 0 (not true at all) to 4 (true nearly all the time), with total scores from 0 to 144; higher scores indicate better QoL.Cronbach's alpha for the FACT-B was 0.951.

Data analysis
SPSS version 26.0 and Mplus version 8.3 were used for data management and analysis.Continuous variables were described as mean ± standard deviation, and categorical variables were described by frequency and percentage.As the dimensions of the four research variables (CRF, SD, PD, and QoL) were not uniform, each variable data were merged at five timepoints, and then standardized and preprocessed.A smoothed line graph was used to visualize the change trajectories of the four variables across different timepoints.Harman's one-factor test was used to test for common method bias, Pearson correlation analysis was used to investigate relationships between the variables at different timepoints, Mplus version 8.3 was used to construct linear growth, and quadratic growth models to explore the variables' development trends 26 .A parallel impact model was established to explore the effects of the intercept and trajectory of change of CRF, SD, and PD on the intercept, and trajectory of change of the QoL.Finally, a cross-lagged panel model was established using Mplus to explore the cross-lagged and timeseries effects of SD, CRF, and PD on QoL.The significance level was set at 0.05.

Participant details
While 648 patients were initially assessed for eligibility, after excluding 109 who did not meet the inclusion criteria, 539 patients were assessed at T1. Subsequently, during T2, T3, T4, and T5 visits, 526, 517, 491, and 448 patients, respectively, were analyzed.Thereafter, as 21 patients were excluded from the analysis, 112 total samples were lost; thus, 427 patients were assessed (Fig. 1).

Description of variables and analysis of development trajectory
Figure 2 shows the average scores for SD, CRF, PD, and QoL at different measurement timepoints, during which each variable showed normal distributions at 0.734 (< 3) and 1.174 (< 10) for maximum absolute kurtosis and skewness, respectively 27 , thus facilitating subsequent analyses.

Correlation analysis
Correlation analysis was used to explore the correlation between the four variables (Table 2).The five measurements of each variable all showed a certain stability.The correlation coefficient between measurements was in the range of 0.341-0.558for CRF, 0.201-0.474for PD, 0.301-0.564for SD, and 0.152-0.478for QoL.The lower triangle of the correlation matrix represents first-order partial; correlation coefficient of each variable at time T1, T1_PD, T1_SD; T1_LQ is the control variable with partial correlation, so the unbiased correlation coefficient is estimated.T1 = within one week after initial cancer diagnosis, T2 = within one week after start of surgical treatment, T3 = within one week after the end of all chemotherapy courses, T4 = six months after the end of chemotherapy, T5 = 12 months after the end of chemotherapy.*P < 0.05, ** P < 0.01.   3 shows the fit indices of the linear and quadratic growth models.The nonlinear growth model has a statistically significant and better fit index than the linear growth model.Hence, there is a non-linear developmental relationship among CRF, PD, SD, and QoL.Table 4 shows the parameter estimation results of the nonlinear latent variable growth model.The initial CRF level was statistically significant and greater than 0 (Intercept = 2.166, P < 0.001), and CRF showed an upward trend over the five surveys (slope = 0.649, P < 0.001), although the growth rate gradually weakened (quadratic = − 0.150, P < 0.001).The variance of the intercept, slope, and quadratic equation were all statistically significant and greater than 0, indicating statistically significant individual differences in the initial CRF level and its developmental speed and trend.
The initial PD level was significantly greater than 0 (intercept = 7.525, P < 0.001), and PD showed a significant weakening trend over the five surveys (slope = − 0.583, P < 0.001), although the weakening speed was gradually moderated (quadratic = 0.051, P < 0.01).The variances of the intercept, slope, and quadratic of PD were all significantly greater than 0 (P < 0.001), indicating statistically significant individual differences in the initial level, linear development trend, and rate of change.
The initial SD level was statistically significant and greater than 0 (Intercept = 0.580, P < 0.001), and SD showed an increasing trend (slope = 0.345, P < 0.001) during the five investigations, although the increase rate gradually dropped (P < 0.001, quadratic = − 0.099), indicating statistically significant differences in the initial level, linear development trend, and rate of change among individuals (P < 0.001).
The initial QoL level was statistically significant and greater than 0 (intercept = 2.393, P < 0.001), and the QoL showed a statistically significant weakening trend during the five surveys (slope = − 0.373, P < 0.001), although the weakening speed was gradually moderated (P < 0.001, quadratic = 0.087), indicating statistically significant differences in the initial level, linear development trend, and rate of change among individuals (P < 0.001).

Parallel growth model
To explore the influence of CRF, PD, and SD on QoL, the parallel impact model of the growth factors among variables was set based on the quadratic growth model (Fig. 3).The model fit indices (χ 2 = 244.873,df = 120, RMSEA = 0.049, CFI = 0.948, TLI = 0.918, SRMR = 0.038) all met the criteria.The initial levels of CRF (coefficient = − 0.233, P < 0.01), PD (coefficient = − 0.296, P < 0.01), and SD (coefficient = − 0.388, P < 0.001) each had a statistically significant negative effect on the initial level of QoL.The linear development rate of PD was statistically significant, and negatively affected the linear development rate of the QoL (coefficient = − 0.305, P < 0.05), and the quadratic development rate of SD negatively affected the quadratic development rate of QoL (coefficient = − 0.391, P < 0.05).The remaining relationship paths were not statistically significant (P > 0.05).

Cross-lagged panel models
The cross-model fitting indices (χ 2 = 267.883,df = 120, RMSEA = 0.054, CFI = 0.935, TLI = 0.900, SRMR = 0.075) showed that all model fit indices meet the standard criteria, indicating that the model is supported by the data and has a good structure (see in Supplementary Table 1).The autoregressive path results show that prior moment CRF, PD, SD, and QoL have a significant positive effect on the autoregressive path of the subsequent moment (P < 0.001), indicating that each variable at the prior moment significantly promotes development at the next moment.
Cross-lagged regression path analysis result (Fig. 4) show that PD within one week after diagnosis (T1) has a significant negative effect on QoL within one week after surgery (T2) (P < 0.05, β = − 0.127).CRF, PD, and SD within one week after surgery (T2) have a significant negative impact on QoL within one week after all chemotherapy sessions (T3) (P < 0.05), with standardized coefficients of − 0.109, − 0.137, and − 0.181 respectively.CRF, PD, and SD within one week after chemotherapy (T3) have a significant negative impact on QoL within six months after chemotherapy (T4) (P < 0.05), with standardized coefficients of − 0.101, − 0.137, and − 0.128 respectively.CRF, PD, and SD within six months after chemotherapy (T4) have a significant negative impact on QoL within twelve months after chemotherapy (T5) (P < 0.05), with standardized coefficients of − 0.130, − 0.113, and − 0.162 respectively.
Additionally, QoL within one week after diagnosis (T1) has a significant negative effect on PD within one week after surgery (T2) (P < 0.05, β = − 0.096).QoL within one week after surgery (T2) has a significant negative effect on CRF and PD within one week after all chemotherapy sessions (T3) (P < 0.05), with standardized coefficients of − 0.097 and − 0.115 respectively.QoL within one week after chemotherapy (T3) has a significant negative effect on SD within six months after chemotherapy (T4) (P < 0.05, β = − 0.091).QoL within six months after chemotherapy (T4) has a significant negative effect on CRF, PD, and SD within twelve months after chemotherapy (T5) (P < 0.05), with standardized coefficients of − 0.106, − 0.145, and − 0.141 respectively.Other paths do not show significant effects between the various timepoints (P > 0.05).

Discussion
The trajectory of CRF and SD changes is similar from T1 to T5.The CRF development trajectory shows an increasing trend and a gradually weakening growth trend.Similarly, the SD development trajectory shows an increasing trend and a gradually weakening growth trend.Within one week after the completion of chemotherapy, CRF and SD are most severe.A potential explanation for this is that when undergoing chemotherapy, along with cancer cells, some normal cells are destroyed, which reduces the body's resistance and causes patients to feel severe physical symptoms 12,24 .As time passes, the cancer-related fatigue and sleep disorders alleviate, but they persist for a long time.Fabi et al. 28 showed that about 50% of patients still experience fatigue, even five years after cancer treatment, and 10-year cancer survivors have high levels of fatigue compared to the general This may be because some individual internal variables regulate the self-perception of CRF and SD in different breast cancer patients.For example, Huang et al. 30 showed that the younger and more educated breast cancer patients feel, the more serious CRF.This suggests that individual factors should be included in the in-depth investigation of CRF and SD formation and development mechanisms.This study revealed that PD trajectories showed a decreasing trend, and the weakening trend is gradually moderated.Significant PD appears at the cancer diagnosis stage, reaching its peak.However, with the advancement of treatment, PD gradually decreases and reaches an adaptive state.This result is consistent with that of previous studies 31,32 and shows that in a clinical situation, even if no special intervention is provided, patients facing stressors will gradually recover.This may be because of changes in patients' resilience levels and emotion regulation 33,34 .The initial PD level has a statistically significant negative effect on initial QoL, indicating that the higher the initial PD, the lower the initial QoL.Furthermore, PD linear growth rate, which is statistically significant, negatively affects the QoL linear development rate, indicating that the faster the PD growth, the faster the QoL decline.Medical staff need to provide interventions such as conducting PD screening and assessment, and managing and providing psychological follow-up during early diagnosis to alleviate breast cancer patients' high PD after diagnosis, thereby improving QoL 30,35 .
The initial CRF, SD, and PD levels significantly negatively affect initial QoL levels, suggesting that if patients already experience high CRF, SD, and PD levels at the time of new diagnosis, their QoL may significantly decrease.Therefore, medical staff should prioritize patients who have significant initial CRF, SD, and PD levels.Cross-lagged model analysis shows that CRF and SD measured at T2, T3, and T4 significantly negatively affect QoL measured at T3, T4, and T5, suggesting that surgery may be a stressor for physical discomfort symptoms.At T2, unpleasant post-surgery symptoms, such as CRF and SD directly affect changes in the next moment as the treatment progresses.PD measured at T1, T2, T3, and T4 significantly negatively affects QoL measured at T2, T3, T4, and T5, indicating that psychological discomfort begins to have a significant longitudinal impact on QoL as early as T1.At T1, PD experienced at the time of diagnosis directly affects changes in QoL at the next moment.Medical staff should adopt various strategies to reduce PD from T1 onwards, while intervening to alleviate CRF and improve SD from T2 onwards.This is of great significance for improving QoL.
This study was conducted during the COVID-19 pandemic, where breast cancer patients already faced issues like CRF, SD, and PD during treatment 36,37 .The spread of the COVID-19 virus undoubtedly aggravated these problems, further affecting the patients' QoL.First, COVID-19 infection can lead to a decrease in the body's immunity, worsening fatigue symptoms severity 38 .Patients might feel even weaker and more powerless.Second, although Rades et al. 39 found that while COVID-19 appeared to have insignificant effects on sleep disorders in breast cancer patients, it is undeniable that symptoms caused by the virus, such as fever and cough, could disturb the patients' sleep.Moreover, PD is common among breast cancer patients during treatment.Breast cancer diagnosis and treatment themselves can exert immense psychological pressure on patients, and the COVID-19 virus threat adds to their fear and anxiety 40 .Patients might worry about the worsening of their condition and fear that it might not be curable, potentially further increasing their PD.At the same time, due to pandemic restrictions, patients might not be able to maintain normal social activities with family and friends, increasing their feelings of loneliness and psychological pressure 41 .Additionally, Baffert et al. 42 found that the QoL for cancer patients was maintained and not affected during the COVID-19 pandemic.However, considering that CRF, SD, and PD interact with each other, they form a vicious cycle that significantly reduces the patients' QoL.Due to the impact of the pandemic, patients might not have been able to receive timely and effective medical services and support, further exacerbating their living difficulties.Although the follow-up was completed as planned, considering the significant impact of COVID-19, the results of this study should be treated with caution.

Study limitations
First, the study variables were all assessed using questionnaire survey methods.Anonymous reporting was adopted to maximally ensure patients' objectivity in the self-assessment of symptoms, but the questionnaire method itself suffers subjective bias that is difficult to overcome, and this may have affected patients' willingness to answer.Future research should adopt implicit methods or combine physiological and neural indicators as measures in laboratory settings to obtain more objective and diverse data sources.Second, as COVID-19 put considerable pressure on patients, which will inevitably affect physical and psychological symptoms, such as causing patients to feel tired as well as experience sleep problems and negative emotions, future research should control for its effects.Furthermore, this study only analyzed the total scores of each scale, which may have resulted in the loss of specific information provided by subscales, thus failing to accurately reflect the actual performance of the assessed individuals in each dimension.Simultaneously, it is not possible to directly compare differences between different dimensions.It is recommended that future research explore the relationships between variables from a dimensional perspective.

Conclusions
This study expands the literature on effects of common physical and psychological symptoms on QoL among breast cancer patients.These findings may help healthcare workers to better understand changes in SD, CRF, PD, and QoL, and their interactions in breast cancer patients, beginning from cancer diagnosis to one year after chemotherapy.The changing CRF and SD trends were consistent, showing an increasing trend that gradually weakened; the changing PD and QoL trends were consistent, both showing a weakening trend that was gradually moderated.Changes in each variable at a previous timepoint affected changes in them at the next timepoint, which suggests that intervention times should be moved forward.In particular, the PD development rate had statistically significant negative effects on the QoL development rate, suggesting that medical staff should provide interventions soon after cancer is diagnosed and actively take various nursing measures to alleviate high PD in breast cancer patients to improve their QoL. https://doi.org/10.1038/s41598-024-59214-0www.nature.com/scientificreports/

Figure 4 .
Figure 4. Cross-lag model path diagram.Note Significant paths are solid lines; Non-statistically significant paths are dashed; T1 = within one week after the initial cancer diagnosis, T2 = within one week after the start of surgical treatment, T3 = within one week after the end of all courses of chemotherapy, T4 = six months after the end of chemotherapy, T5 = 12 months after the end of chemotherapy; *P < 0.05; **P < 0.01; ***P < 0.001.

Table 1 .
Demographic and clinical characteristics.

Table 2 .
Correlation analysis and partial correlation matrix.The triangle on the correlation matrix represents the Pearson correlation coefficient.

Table 3 .
Fit indices of linear and quadratic latent variable growth models.